GLP-1-induced alterations in the glucose-stimulated insulin secretory dose-response curve

Citation
A. Brandt et al., GLP-1-induced alterations in the glucose-stimulated insulin secretory dose-response curve, AM J P-ENDO, 281(2), 2001, pp. E242-E247
Citations number
33
Categorie Soggetti
Endocrinology, Nutrition & Metabolism
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM
ISSN journal
01931849 → ACNP
Volume
281
Issue
2
Year of publication
2001
Pages
E242 - E247
Database
ISI
SICI code
0193-1849(200108)281:2<E242:GAITGI>2.0.ZU;2-A
Abstract
The present study was undertaken to establish in normal volunteers the alte rations in beta -cell responsiveness to glucose associated with a constant infusion of glucagon-like peptide-1 (GLP-1) or a pretreatment infusion for 60 min. A high-dose graded glucose infusion protocol was used to explore th e dose-response relationship between glucose and insulin secretion. Studies were performed in 10 normal volunteers, and insulin secretion rates (ISR) were calculated by deconvolution of peripheral C-peptide levels by use of a two-compartmental model that utilized mean kinetic parameters. During the saline study, from 5 to 15 mM glucose, the relationship between glucose and ISR was linear. Constant GLP-1 infusion (0.4 pmol.kg(-1).min(-1)) shifted the dose-response curve to the left, with an increase in the slope of this curve from 5 to 9 mM glucose from 71.0 +/- 12.4 pmol.min(-1).mM(-1) during the saline study to 241.7 +/- 36.6 pmol.min(-1).mM(-1) during the constant GLP-1 infusion (P< 0.0001). GLP-1 consistently stimulated a >200% increase in ISR at each 1 mM glucose interval, maintaining plasma glucose at,10 mM ( P< 0.0007). Pretreatment with GLP-1 for 60 min resulted in no significant p riming of the <beta>-cell response to glucose (P = 0.2). Insulin clearance rates were similar in all three studies at corresponding insulin levels. Th ese studies demonstrate that physiological levels of GLP-1 stimulate glucos e-induced insulin secretion in a linear manner, with a consistent increase in ISR at each 1 mM glucose interval, and that they have no independent eff ect on insulin clearance and no priming effect on subsequent insulin secret ory response to glucose.